Bundle: Principles of Modern Chemistry, Loose-leaf Version, 8th + LMS Integrated for OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card
Bundle: Principles of Modern Chemistry, Loose-leaf Version, 8th + LMS Integrated for OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card
8th Edition
ISBN: 9781305786950
Author: David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher: Cengage Learning
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Chapter 7, Problem 37AP

trans-Cyclodecene boils at 193 ° C, but cis-cyclodecene boils at 195.6 ° C . Write structural formulas for these two compounds.

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Are the products of the given reaction correct?  Why or why not?
The question below asks why the products shown are NOT the correct products.  I asked this already, and the person explained why those are the correct products, as opposed to what we would think should be the correct products.  That's the opposite of what the question was asking.  Why are they not the correct products? A reaction mechanism for how we arrive at the correct products is requested ("using key intermediates").  In other words, why is HCl added to the terminal alkene rather than the internal alkene?
My question is whether HI adds to both double bonds, and if it doesn't, why not?

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Bundle: Principles of Modern Chemistry, Loose-leaf Version, 8th + LMS Integrated for OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card

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Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License